Table 5.
Authors | Year | Intervention (patient number) | Outcome(s) | Results |
---|---|---|---|---|
Narasimhan et al. 163 | 2017 | Cholecalciferol 6 lac IU i.m. (n = 30 per group) |
|
Stroke outcome significantly improved in vitamin D deficient—but not insufficient—patients once supplemented (mean 6.39 ± 4.56 vs. 2.50 ± 2.20; P < 0.001) |
Sari et al. 164 | 2018 | Cholecalciferol 300 000 IU i.m. (n = 36 per group) |
|
3.09 ± 0.99 vs. 3.34 ± 5.28; P = 0.794
2.34 ± 1.31 vs. 1.60 ± 1.16; P = 0.018 59.18 ± 22.15 vs. 41.87 ± 20.42; P = 0.002 38.72 ± 14.14 vs. 24.75 ± 14.76; P < 0.001 |
Momosaki et al. 165 | 2019 | Cholecalciferol 2 000 IU/die i.m. (n = 49/48) |
|
19 ± 15 vs. 20 ± 13; P = 0.480
27%–20% vs. 25%–18%; P = 0.770;0.740 19%–20% vs. 23%–20%; P = 0.770;0.600 |
Rist et al. 166 from the VITAL study | 2021 | Cholecalciferol 2 000 IU/die i.m. in primary prevention (n = 104/93 per group) |
Nagi scale
Rosow-Breslau scale Katz AD scale |
OR 1.01 [95% CI 0.52–1.97]
OR 0.92 [95% CI 0.59–1.67] OR 1.03 [95% CI 0.31–3.42] |
Torrisi et al. 167 | 2021 | Cholecalciferol 2 000 IU/die i.m. (n = 15/14) per group) |
MADRS
FIM GSE (all at 12 weeks) |
Both groups improved mood and functional recovery independently of vitamin D supplementation |
Wang et al. 168 | 2021 | Cholecalciferol 600 IU/die i.m. (n = 72/51 per group) |
mRS
FSS (both at 3 months) |
FSS and mRS significanlty lowered in the supplementation group (P < 0.01 for both) |
CI, confidence interval; OR, odds ratio; SSS, Scandinavian Stroke Scale; BRS, Brunnstrom recovery staging; FAS, functional ambulation scale; MBI, modified Barthel index; BBS, Berg balance scale; MADRS, Montgomery Aasberg depression rating scale; FIM, functional independent measures; GSE, general self-efficacy; mRS, modified Rankin score; FSS, fatigue severity scale.